Protective action of EGCG against anticancer drugs MMS and CP

T. Beg, Y. Siddique, G. Ara, J. Gupta, Mohammad Afzal
{"title":"Protective action of EGCG against anticancer drugs MMS and CP","authors":"T. Beg, Y. Siddique, G. Ara, J. Gupta, Mohammad Afzal","doi":"10.5580/19b4","DOIUrl":null,"url":null,"abstract":"This experiment was conducted in order to assess the antigenotoxicity potential of Epigallocatechin-3-gallate (EGCG), a catechin, against genotoxicity induced by anticancer drugs, Methyl methanesulphonate (MMS) and cyclophosphamide (CP), in the form of chromosomal aberrations (CAs) and sister chromatid exchanges (SCEs). These drugs were used at 60 M and 0.16 g/ml respectively along with EGCG at 10, 20, and 30 M in cultured human lymphocyte chromosomes. EGCG significantly reduced the genotoxic damage induced by the two drugs both in the presence and absence of metabolic activation system (S9 mix), although with greater effectiveness in the presence of metabolic activation.","PeriodicalId":22523,"journal":{"name":"The Internet Journal of Pharmacology","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2008-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet Journal of Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/19b4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

This experiment was conducted in order to assess the antigenotoxicity potential of Epigallocatechin-3-gallate (EGCG), a catechin, against genotoxicity induced by anticancer drugs, Methyl methanesulphonate (MMS) and cyclophosphamide (CP), in the form of chromosomal aberrations (CAs) and sister chromatid exchanges (SCEs). These drugs were used at 60 M and 0.16 g/ml respectively along with EGCG at 10, 20, and 30 M in cultured human lymphocyte chromosomes. EGCG significantly reduced the genotoxic damage induced by the two drugs both in the presence and absence of metabolic activation system (S9 mix), although with greater effectiveness in the presence of metabolic activation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
EGCG对抗癌药物MMS和CP的保护作用
本实验旨在研究儿茶素表没食子儿茶素-3-没食子酸酯(EGCG)对抗肿瘤药物甲基磺酸钠(MMS)和环磷酰胺(CP)以染色体畸变(CAs)和姐妹染色单体交换(SCEs)形式诱导的遗传毒性。这些药物分别在60M和0.16g/ml浓度下与EGCG在10、20和30M浓度下作用于培养的人淋巴细胞染色体。无论是否存在代谢激活系统(S9混合物),EGCG都显著降低了两种药物引起的基因毒性损伤,尽管在存在代谢激活系统时效果更大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Acute And Subacute Toxicity Of Aqueous Extract Of Abrus Precatorius Seed In Wister Rats Artemisinin Combination Therapies; Safe Or Not Safe ? An Antibacterial Drug Utilization Study at Surgical Units of Shree Sayaji General Hospital, Vadodara, Gujarat, India Rational Use of Drugs and Irrational Drug Combinations Evaluation Of Antiulcer Activity Of Ocimum Sanctum And Its Mechanism In Animal Models
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1